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[成人急性淋巴细胞白血病首次缓解后骨髓移植与维持化疗的长期生存比较]

[Comparison of long-term survival between bone marrow transplantation and maintenance chemotherapy for adult acute lymphoblastic leukemia in first remission].

作者信息

Suzuki N, Koike T, Furukawa T, Niwano H, Maruyama S, Narita M, Takizawa J, Sato N, Hashimoto S, Nikkuni K, Toba K, Kishi K, Takahashi M, Aizawa Y, Shibata A

机构信息

Division of Bone Marrow Transplanation, Niigata University Medical Hospital, Japan.

出版信息

Rinsho Ketsueki. 1997 Feb;38(2):95-9.

PMID:9059062
Abstract

To clarify the efficacy of allogeneic bone marrow transplantation (BMT) for adult ALL in first remission we retrospectively studied long-term outcomes of adult ALL patients of age between 15 and 44 years who were treated in our institute from 1980 to 1990. In this period thirteen patients with HLA compatible donors were offered allogeneic BMT during the first remission, while 16 patients without HLA-compatible donor were treated with maintenance chemotherapy (Cancer Chemoth Pharmacology 33:359-365, 1994). Patient and disease characteristics (age, leukocyte count at presentation, immunophenotype, Ph1 chromosome, and duration to first remission) in the two groups were not significantly different (chi-square test p > 0.1). As causes of treatment failure, relapse was 90% for chemotherapy while relapse and therapy-related death were 67% and 33%, respectively, for transplantation. The leukemia-free survival (LFS) rates at 10 years were 52 +/- 13% for transplantation and 30 +/- 11% for chemotherapy (P > 0.2, g-Wilcoxon, Logrank). The 10-year-LFS rates of Ph1-negative patients of 15 to 29 year-old were 67 +/- 15% for transplantation (n = 9) and 62 +/- 15% for chemotherapy (n = 8) (P > 0.9). Although the present data are derived from a non randomized retrospective study and a relatively small number of patients, this study revealed no superiority of BMT over chemotherapy for the prolongation of first remission in adult ALL, especially, in a standard risk group such as young patients without Ph1 chromosome.

摘要

为明确异基因骨髓移植(BMT)对首次缓解期成人急性淋巴细胞白血病(ALL)的疗效,我们回顾性研究了1980年至1990年在我院接受治疗的15至44岁成人ALL患者的长期预后。在此期间,13例有人类白细胞抗原(HLA)相匹配供者的患者在首次缓解期接受了异基因BMT,而16例无HLA相匹配供者的患者接受了维持化疗(《癌症化疗药理学》33:359 - 365,1994)。两组患者及疾病特征(年龄、初诊时白细胞计数、免疫表型、Ph1染色体以及首次缓解持续时间)无显著差异(卡方检验p>0.1)。作为治疗失败的原因,化疗组复发率为90%,而移植组复发率和治疗相关死亡率分别为67%和33%。移植组10年无白血病生存率(LFS)为52±13%,化疗组为30±11%(P>0.2,g - Wilcoxon检验,对数秩检验)。15至29岁Ph1阴性患者的10年LFS率,移植组为67±15%(n = 9),化疗组为62±15%(n = 8)(P>0.9)。尽管目前的数据来自非随机回顾性研究且患者数量相对较少,但本研究显示,对于延长成人ALL的首次缓解期,尤其是在年轻无Ph1染色体等标准风险组中,BMT并不优于化疗。

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